Current partner codePEPTIDESDE
ApprovedClinical / approved drugIntravenousEvidence 4/5

Vasopressin

Also known as: Vasostrict, ADH, AVP

Vasopressin activates V1a receptors on vascular smooth muscle to cause vasoconstriction and V2 receptors in the renal collecting duct to drive aquaporin-2-mediated water reabsorption, raising blood pressure and concentrating urine.

This page is a structured profile. Narrative evidence, dosing context and FAQs live on the research guide — not duplicated here as a second full article.

Illustrative intravenous database profile for Vasopressin
Illustrative profileIntravenous
Database profileApproved
VasopressinClinical / approved drug
Drug class
Endogenous nonapeptide hormone; vasopressor / antidiuretic hormone
Primary targets
V1a receptor, V2 receptor, V1b (V3) receptor
Dose reference
Label reference ranges (not recommendations): post-cardiotomy shock 0.03-0.1 units/min IV; septic shock 0.01-0.07 units/min IV continuous infusion
Half-life
Short; apparent half-life roughly 10 minutes or less per the Vasostrict label
Developer / origin
Vasostrict product marketed by Par Pharmaceutical; vasopressin first synthesized by Vincent du Vigneaud (1950s)
Reference year
2014
Evidence score
4/5 - Approved drug with strong pharmacologic evidence, modest mortality data

Approved uses

  • Vasodilatory shock in adults (e.g., post-cardiotomy or septic shock) who remain hypotensive despite fluids and catecholamines
Evidence 4/5

Approved drug with strong pharmacologic evidence, modest mortality data

Vasopressin (Vasostrict) is FDA-approved as an intravenous vasopressor for vasodilatory shock, backed by a clear FDA label and the randomized VASST trial. The label and pharmacology robustly support its blood-pressure and antidiuretic effects, but VASST did not show a significant overall survival benefit, so hard-outcome evidence is more limited.

Investigational compound with human randomized or phase 2/3 evidence.

Evidence basis

  • FDA Vasostrict prescribing information defining the vasodilatory shock indication, IV route and dosing ranges
  • VASST randomized controlled trial (n=778, NEJM 2008) of vasopressin vs norepinephrine in septic shock
  • Peer-reviewed pharmacology establishing V1a vasoconstriction and V2 antidiuretic mechanisms
  • Decades of established clinical use including historical central diabetes insipidus treatment

How to read this entry

Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.

Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.

Vasopressin guides

Read the matching guide or adjacent research pages for more context.

Peptide calculators

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